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Circulating Coding and Long Non-Coding RNAs as Potential Biomarkers of Idiopathic Pulmonary Fibrosis

Background: Idiopathic Pulmonary Fibrosis (IPF) is a chronic degenerative disease with a median survival of 2–5 years after diagnosis. Therefore, IPF patient identification represents an important and challenging clinical issue. Current research is still searching for novel reliable non-invasive bio...

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Detalles Bibliográficos
Autores principales: Di Mauro, Stefania, Scamporrino, Alessandra, Fruciano, Mary, Filippello, Agnese, Fagone, Evelina, Gili, Elisa, Scionti, Francesca, Purrazzo, Giacomo, Di Pino, Antonino, Scicali, Roberto, Di Martino, Maria Teresa, Malaguarnera, Roberta, Malatino, Lorenzo, Purrello, Francesco, Vancheri, Carlo, Piro, Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709007/
https://www.ncbi.nlm.nih.gov/pubmed/33233868
http://dx.doi.org/10.3390/ijms21228812